Works matching AU Hankins, Jane S.

Results: 142

Recruitment Strategies in the Integration of Mobile Health Into Sickle Cell Disease Care to Increase Hydroxyurea Utilization Study (meSH): Multicenter Survey Study.

Published in:

JMIR Formative Research, 2024, v. 8, p. 1, doi. 10.2196/48767

By:

Nwosu, Chinonyelum;
Khan, Hamda;
Masese, Rita;
Nocek, Judith M;
Gollan, Siera;
Varughese, Taniya;
Bourne, Sarah;
Clesca, Cindy;
Jacobs, Sara R;
Baumann, Ana;
Klesges, Lisa M;
Shah, Nirmish;
Hankins, Jane S;
Smeltzer, Matthew P

Publication type:

Article

Transition Readiness Assessment for Sickle Cell Patients: A Quality Improvement Project.

Published in:

Journal of Clinical Outcomes Management, 2014, v. 21, n. 6, p. 263

By:

Porte, Jerlym S.;
Carroll, Yvonne M.;
Anderson, Sheila;
Lavoie Jr., Paul T.;
Hamilton, Latacha;
Johnson, Margery;
Hankins, Jane S.

Publication type:

Article

Transition Readiness Assessment for Sickle Cell Patients: A Quality Improvement Project.

Published in:

2012

By:

Porte, Jerlym S.;
Carroll, Yvonne M.;
Anderson, Sheila;
Lavoie Jr., Paul T.;
Hamilton, Latacha;
Johnson, Margery;
Hankins, Jane S.

Publication type:

Journal Article

Mortality in adults with sickle cell disease: Results from the sickle cell disease implementation consortium (SCDIC) registry.

Published in:

American Journal of Hematology, 2024, v. 99, n. 5, p. 900, doi. 10.1002/ajh.27279

By:

Njoku, Franklin;
Pugh, Norma;
Brambilla, Donald;
Kroner, Barbara;
Shah, Nirmish;
Treadwell, Marsha;
Gibson, Robert;
Hsu, Lewis L.;
Gordeuk, Victor R.;
Glassberg, Jeffrey;
Hankins, Jane S.;
Kutlar, Abdullah;
King, Allison A.;
Kanter, Julie

Publication type:

Article

Comparative pharmacovigilance assessment of adverse events associated with the use of hydroxyurea, L‐glutamine, voxelotor, and crizanlizumab in sickle cell disease.

Published in:

American Journal of Hematology, 2024, v. 99, n. 2, p. E37, doi. 10.1002/ajh.27153

By:

Chen, Ming;
Hankins, Jane S.;
Zhang, Min;
Ataga, Kenneth I.

Publication type:

Article

Academic Performance of Children With Sickle Cell Disease in the United States: A Meta-Analysis.

Published in:

Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.786065

By:

Heitzer, Andrew M.;
Hamilton, Latacha;
Stafford, Claire;
Gossett, Jeffrey;
Ouellette, Lara;
Trpchevska, Ana;
King, Allison A.;
Kang, Guolian;
Hankins, Jane S.

Publication type:

Article

Addressing challenges of clinical trials in acute pain: The Pain Management of Vaso-occlusive Crisis in Children and Young Adults with Sickle Cell Disease Study.

Published in:

Clinical Trials, 2016, v. 13, n. 4, p. 409, doi. 10.1177/1740774516636573

By:

Nottage, Kerri A.;
Hankins, Jane S.;
Faughnan, Lane G.;
James, Dustin M.;
Richardson, Julie;
Christensen, Robbin;
Kang, Guolian;
Smeltzer, Matthew;
Cancio, Maria I.;
Wang, Winfred C.;
Anghelescu, Doralina L.

Publication type:

Article

Optimizing haematopoietic stem and progenitor cell apheresis collection from plerixafor‐mobilized patients with sickle cell disease.

Published in:

British Journal of Haematology, 2022, v. 198, n. 4, p. 740, doi. 10.1111/bjh.18311

By:

Sharma, Akshay;
Leonard, Alexis;
West, Kamille;
Gossett, Jeffrey M.;
Uchida, Naoya;
Panch, Sandhya;
Stroncek, David;
Poston, Leigh;
Akel, Salem;
Hankins, Jane S.;
Fitzhugh, Courtney;
Hsieh, Matthew M.;
Kang, Guolian;
Tisdale, John F.;
Weiss, Mitchell J.;
Zheng, Yan

Publication type:

Article

Neurocognitive risk in sickle cell disease: Utilizing neuropsychology services to manage cognitive symptoms and functional limitations.

Published in:

British Journal of Haematology, 2022, v. 197, n. 3, p. 260, doi. 10.1111/bjh.18041

By:

Longoria, Jennifer N.;
Heitzer, Andrew M.;
Hankins, Jane S.;
Trpchevska, Ana;
Porter, Jerlym S.

Publication type:

Article

Bridging the implementation gap in medication adherence. If you build it, will they come?

Published in:

British Journal of Haematology, 2022, v. 196, n. 1, p. 17, doi. 10.1111/bjh.17953

By:

Hankins, Jane S.;
Klesges, Lisa M.

Publication type:

Article

Time to rethink haemoglobin threshold guidelines in sickle cell disease.

Published in:

British Journal of Haematology, 2021, v. 195, n. 4, p. 518, doi. 10.1111/bjh.17578

By:

Ballas, Samir K.;
Kuypers, Frans A.;
Gordeuk, Victor R.;
Hankins, Jane S.;
Thompson, Alexis A.;
Vichinsky, Elliott

Publication type:

Article

Hydroxyurea treatment and neurocognitive functioning in sickle cell disease from school age to young adulthood.

Published in:

British Journal of Haematology, 2021, v. 195, n. 2, p. 256, doi. 10.1111/bjh.17687

By:

Heitzer, Andrew M.;
Longoria, Jennifer;
Okhomina, Victoria;
Wang, Winfred C.;
Raches, Darcy;
Potter, Brian;
Jacola, Lisa M.;
Porter, Jerlym;
Schreiber, Jane E.;
King, Allison A.;
Kang, Guolian;
Hankins, Jane S.

Publication type:

Article

Generalization of a genetic risk score for time to first albuminuria in children with sickle cell anaemia: SCCRIP cohort study results.

Published in:

British Journal of Haematology, 2021, v. 194, n. 2, p. 469, doi. 10.1111/bjh.17647

By:

Rashkin, Sara R.;
Rampersaud, Evadnie;
Kang, Guolian;
Ataga, Kenneth I.;
Hankins, Jane S.;
Wang, Winfred;
Estepp, Jeremie H.;
Weiss, Mitchell J.;
Lebensburger, Jeffrey;
Zahr, Rima S.

Publication type:

Article

What drives transcranial Doppler velocity improvement in paediatric sickle cell anaemia: analysis from the Sickle Cell Clinical Research and Intervention Program (SCCRIP) longitudinal cohort study.

Published in:

British Journal of Haematology, 2021, v. 194, n. 2, p. 463, doi. 10.1111/bjh.17620

By:

Estepp, Jeremie H.;
Cong, Ze;
Agodoa, Irene;
Kang, Guolian;
Ding, Juan;
McCarville, M. Beth;
Hankins, Jane S.;
Wang, Winfred C.

Publication type:

Article

Cognitive performance as a predictor of healthcare transition in sickle cell disease.

Published in:

British Journal of Haematology, 2021, v. 192, n. 6, p. 1082, doi. 10.1111/bjh.17351

By:

Saulsberry‐Abate, Anjelica C.;
Partanen, Marita;
Porter, Jerlym S.;
Podila, Pradeep S. B.;
Hodges, Jason R.;
King, Allison A.;
Wang, Winfred C.;
Schreiber, Jane E.;
Zhao, Xiwen;
Kang, Guolian;
Jacola, Lisa M.;
Hankins, Jane S.

Publication type:

Article

Association between hydroxycarbamide exposure and neurocognitive function in adolescents with sickle cell disease.

Published in:

British Journal of Haematology, 2020, v. 189, n. 6, p. 1192, doi. 10.1111/bjh.16519

By:

Partanen, Marita;
Kang, Guolian;
Wang, Winfred C.;
Krull, Kevin;
King, Allison A.;
Schreiber, Jane E.;
Porter, Jerlym S.;
Hodges, Jason;
Hankins, Jane S.;
Jacola, Lisa M.

Publication type:

Article

Ventricular global longitudinal strain is altered in children with sickle cell disease.

Published in:

British Journal of Haematology, 2018, v. 183, n. 5, p. 796, doi. 10.1111/bjh.15607

By:

Whipple, Nicholas S.;
Naik, Ronak J.;
Kang, Guolian;
Moen, Joseph;
Govindaswamy, Sarala D.;
Fowler, James A.;
Dowdy, Jolanta;
Penkert, Rhiannon;
Joshi, Vijaya M.;
Hankins, Jane S.

Publication type:

Article

Hydroxycarbamide treatment and brain MRI/MRA findings in children with sickle cell anaemia.

Published in:

British Journal of Haematology, 2016, v. 175, n. 2, p. 331, doi. 10.1111/bjh.14235

By:

Nottage, Kerri A.;
Ware, Russell E.;
Aygun, Banu;
Smeltzer, Matthew;
Kang, Guolian;
Moen, Joseph;
Wang, Winfred C.;
Hankins, Jane S.;
Helton, Kathleen J.

Publication type:

Article

The effect of hydroxcarbamide therapy on survival of children with sickle cell disease.

Published in:

British Journal of Haematology, 2013, v. 161, n. 6, p. 852, doi. 10.1111/bjh.12323

By:

Lopes de Castro Lobo, Clarisse;
Pinto, Jorge F. C.;
Nascimento, Emilia M.;
Moura, Patricia G.;
Cardoso, Gilberto P.;
Hankins, Jane S.

Publication type:

Article

Protection from sickle cell retinopathy is associated with elevated HbF levels and hydroxycarbamide use in children.

Published in:

British Journal of Haematology, 2013, v. 161, n. 3, p. 402, doi. 10.1111/bjh.12238

By:

Estepp, Jeremie H.;
Smeltzer, Matthew P.;
Wang, Winfred C.;
Hoehn, Mary E.;
Hankins, Jane S.;
Aygun, Banu

Publication type:

Article

Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia.

Published in:

British Journal of Haematology, 2012, v. 157, n. 2, p. 240, doi. 10.1111/j.1365-2141.2012.09061.x

By:

Flanagan, Jonathan M.;
Steward, Shirley;
Howard, Thad A.;
Mortier, Nicole A.;
Kimble, Amy C.;
Aygun, Banu;
Hankins, Jane S.;
Neale, Geoffrey A.;
Ware, Russell E.

Publication type:

Article

Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.

Published in:

British Journal of Haematology, 2012, v. 156, n. 2, p. 259, doi. 10.1111/j.1365-2141.2011.08916.x

By:

Ngo, Duyen A.;
Aygun, Banu;
Akinsheye, Idowu;
Hankins, Jane S.;
Bhan, Ishir;
Luo, Hong Y.;
Steinberg, Martin H.;
Chui, David H. K.

Publication type:

Article

Burden of Aging: Health Outcomes Among Adolescents and Young Adults With Sickle Cell Disease.

Published in:

HemaSphere, 2023, v. 7, n. 8, p. 1, doi. 10.1097/HS9.0000000000000930

By:

Howell, Kristen E.;
Pugh, Norma;
Longoria, Jennifer;
Shah, Nirmish;
Kutlar, Abdullah;
Gordeuk, Victor R.;
King, Allison A.;
Glassberg, Jeffrey;
Kayle, Mariam;
Melvin, Cathy;
Treadwell, Marsha;
Hankins, Jane S.;
Porter, Jerlym S.

Publication type:

Article

Caregiver and provider perspectives on developmental services for children with sickle cell disease: a mixed methods analysis.

Published in:

Frontiers in Pediatrics, 2025, p. 1, doi. 10.3389/fped.2025.1530457

By:

Tamboli, Mollie;
MacArthur, Erin;
Collins, Natalie;
Kang, Eunyoung;
Fernandez, Maria;
Porter, Jerlym S.;
Conklin, Heather M.;
King, Allison A.;
Hankins, Jane S.;
Heitzer, Andrew M.

Publication type:

Article

Awareness, access, and communication: provider perspectives on early intervention services for children with sickle cell disease.

Published in:

Frontiers in Pediatrics, 2024, p. 1, doi. 10.3389/fped.2024.1366522

By:

Heitzer, Andrew M.;
MacArthur, Erin;
Tamboli, Mollie;
Wilson, Ashley;
Hankins, Jane S.;
Hoyt, Catherine R.

Publication type:

Article

Association between hospital admissions and healthcare provider communication for individuals with sickle cell disease.

Published in:

Hematology, 2020, v. 25, n. 1, p. 229, doi. 10.1080/16078454.2020.1780737

By:

Cronin, Robert M.;
Yang, Manshu;
Hankins, Jane S.;
Byrd, Jeannie;
Pernell, Brandi M.;
Kassim, Adetola;
Adams-Graves, Patricia;
Thompson, Alexis A.;
Kalinyak, Karen;
DeBaun, Michael;
Treadwell, Marsha

Publication type:

Article

Risk factors for hospitalizations and readmissions among individuals with sickle cell disease: results of a U.S. survey study.

Published in:

Hematology, 2019, v. 24, n. 1, p. 189, doi. 10.1080/16078454.2018.1549801

By:

Cronin, Robert M.;
Hankins, Jane S.;
Byrd, Jeannie;
Pernell, Brandi M.;
Kassim, Adetola;
Adams-Graves, Patricia;
Thompson, Alexis;
Kalinyak, Karen;
DeBaun, Michael;
Treadwell, Marsha

Publication type:

Article

Risk factors for hospitalizations and readmissions among individuals with sickle cell disease: results of a U.S. survey study.

Published in:

Hematology, 2019, v. 24, n. 1, p. 189, doi. 10.1080/16078454.2018.1549801

By:

Cronin, Robert M.;
Hankins, Jane S.;
Byrd, Jeannie;
Pernell, Brandi M.;
Kassim, Adetola;
Adams-Graves, Patricia;
Thompson, Alexis;
Kalinyak, Karen;
DeBaun, Michael;
Treadwell, Marsha

Publication type:

Article

Modifying factors of the health belief model associated with missed clinic appointments among individuals with sickle cell disease.

Published in:

Hematology, 2018, v. 23, n. 9, p. 683, doi. 10.1080/10245332.2018.1457200

By:

Cronin, Robert M.;
Hankins, Jane S.;
Byrd, Jeannie;
Pernell, Brandi M.;
Kassim, Adetola;
Adams-Graves, Patricia;
Thompson, Alexis A.;
Kalinyak, Karen;
DeBaun, Michael R.;
Treadwell, Marsha

Publication type:

Article

Removal of Arterial Vessel Contributions in Susceptibility-Weighted Images for Quantification of Normalized Visible Venous Volume in Children with Sickle Cell Disease.

Published in:

Journal of Healthcare Engineering, 2017, p. 1, doi. 10.1155/2017/5369385

By:

Winchell, Adam M.;
Song, Ruitian;
Loeffler, Ralf B.;
Wang, Winfred C.;
Hankins, Jane S.;
Helton, Kathleen J.;
Hillenbrand, Claudia M.

Publication type:

Article

Empirically derived profiles of neurocognitive functioning in youth and young adults with sickle cell disease.

Published in:

Journal of Pediatric Psychology, 2024, v. 49, n. 9, p. 605, doi. 10.1093/jpepsy/jsae029

By:

Ellison, Vinkrya;
Berlin, Kristoffer S;
Longoria, Jennifer;
Potter, Brian;
Raches, Darcy;
Hankins, Jane S;
Takemoto, Clifford;
Heitzer, Andrew M

Publication type:

Article

Internalizing Symptoms in Adolescents With Sickle Cell Disease.

Published in:

Journal of Pediatric Psychology, 2023, v. 48, n. 1, p. 91, doi. 10.1093/jpepsy/jsac068

By:

Heitzer, Andrew M;
Longoria, Jennifer;
Porter, Jerlym S;
MacArthur, Erin;
Potter, Brian;
Ding, Juan;
Gossett, Jeffrey;
Kang, Guolian;
Hankins, Jane S

Publication type:

Article

Adaptive Functioning in Children and Adolescents With Sickle Cell Disease.

Published in:

2022

By:

Trpchevska, Ana;
Longoria, Jennifer;
Okhomina, Victoria;
Raches, Darcy;
Potter, Brian;
Kang, Guolian;
Heitzer, Andrew M;
Hankins, Jane S

Publication type:

journal article

Nocturnal Enuresis in Sickle Cell: Sociodemographic, Medical, and Quality of Life Factors.

Published in:

2022

By:

Porter, Jerlym S;
Paladino, Andrew J;
Russell, Kathryn;
Rupff, Rebecca;
Griffith, Jamilla;
Mai, Yujiao;
Zhang, Hui;
Hankins, Jane S;
Wang, Winfred C

Publication type:

journal article

Empirically Derived Profiles of Health-Related Quality of Life in Youth and Young Adults with Sickle Cell Disease.

Published in:

2021

By:

Keenan, Mary E;
Loew, Megan;
Berlin, Kristoffer S;
Hodges, Jason;
Alberts, Nicole M;
Hankins, Jane S;
Porter, Jerlym S

Publication type:

journal article

Pediatric to Adult Care Transition: Perspectives of Young Adults With Sickle Cell Disease.

Published in:

2017

By:

Porter, Jerlym S.;
Wesley, Kimberly M.;
Rupff, Rebecca J.;
Hankins, Jane S.;
Zhao, Mimi S

Publication type:

journal article

Progression of central nervous system disease from pediatric to young adulthood in sickle cell anemia.

Published in:

Experimental Biology & Medicine, 2021, v. 246, n. 23, p. 2473, doi. 10.1177/15353702211035778

By:

Champlin, Grace;
Hwang, Scott N;
Heitzer, Andrew;
Ding, Juan;
Jacola, Lisa;
Estepp, Jeremie H;
Wang, Winfred;
Ataga, Kenneth I;
Owens, Curtis L;
Newman, Justin;
King, Allison A;
Davis, Robert;
Kang, Guolian;
Hankins, Jane S

Publication type:

Article

A Novel One‐Sample Mendelian Randomization Approach for Count‐Type Outcomes That Is Robust to Correlated and Uncorrelated Pleiotropic Effects.

Published in:

Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22602

By:

Liyanage, Janaka S. S.;
Hankins, Jane S.;
Estepp, Jeremie H.;
Srivastava, Deokumar;
Rashkin, Sara R.;
Takemoto, Clifford;
Li, Yun;
Cui, Yuehua;
Mori, Motomi;
Weiss, Mitchell J.;
Kang, Guolian

Publication type:

Article

Hydroxyurea Use After Transitions of Care Among Young Adults With Sickle Cell Disease and Tennessee Medicaid Insurance.

Published in:

JAMA Network Open, 2021, v. 4, n. 10, p. e2128971, doi. 10.1001/jamanetworkopen.2021.28971

By:

Mathias, Joacy G.;
Nolan, Vikki G.;
Klesges, Lisa M.;
Badawy, Sherif M.;
Cooper, William O.;
Hankins, Jane S.;
Smeltzer, Matthew P.

Publication type:

Article

Hypothesis: Low Vitamin A and D Levels Worsen Clinical Outcomes When Children with Sickle Cell Disease Encounter Parvovirus B19.

Published in:

Nutrients, 2022, v. 14, n. 16, p. 3415, doi. 10.3390/nu14163415

By:

Penkert, Rhiannon R.;
Azul, Melissa;
Sealy, Robert E.;
Jones, Bart G.;
Dowdy, Jola;
Hayden, Randall T.;
Tang, Li;
Ross, A. Catharine;
Hankins, Jane S.;
Hurwitz, Julia L.

Publication type:

Article

Depression, sleep and pain affect instrumental activities of daily living through cognitive functioning in adults with sickle cell disease: A report from the Sickle Cell Disease Implementation Consortium.

Published in:

British Journal of Haematology, 2025, v. 206, n. 3, p. 944, doi. 10.1111/bjh.19881

By:

Longoria, Jennifer N.;
Howell, Kristen E.;
Porter, Jerlym S.;
Treadwell, Marsha;
King, Allison A.;
Gordeuk, Victor;
Shah, Nirmish;
Abrams, Christina M.;
McCuskee, Sarah;
Gollan, Siera;
Hankins, Jane S.;
Heitzer, Andrew M.

Publication type:

Article

Provider prescription of hydroxyurea in youth and adults with sickle cell disease: A review of prescription barriers and facilitators.

Published in:

British Journal of Haematology, 2023, v. 203, n. 5, p. 712, doi. 10.1111/bjh.19099

By:

Pizzo, Alex;
Porter, Jerlym S.;
Carroll, Yvonne;
Burcheri, Adam;
Smeltzer, Matthew P.;
Beestrum, Molly;
Nwosu, Chinonyelum;
Badawy, Sherif M.;
Hankins, Jane S.;
Klesges, Lisa M.;
Alberts, Nicole M.

Publication type:

Article

Characterising the prevalence of overweight and obese status among adults with sickle cell disease.

Published in:

British Journal of Haematology, 2023, v. 200, n. 5, p. 633, doi. 10.1111/bjh.18548

By:

Ibemere, Stephanie O.;
Oyedeji, Charity I.;
Preiss, Liliana;
Van Althuis, Laura E.;
Hankins, Jane S.;
Azul, Melissa;
Burns, Ebony N.;
Glassberg, Jeffrey;
Hagar, Ward;
Hussain, Faiz;
King, Allison;
Melvin, Cathy;
Myers, John;
Snyder, Angela;
Shah, Nirmish;
Tanabe, Paula

Publication type:

Article

Working memory and school readiness in preschool children with sickle cell disease compared to demographically matched controls.

Published in:

British Journal of Haematology, 2023, v. 200, n. 3, p. 358, doi. 10.1111/bjh.18507

By:

Heitzer, Andrew M.;
Schreiber, Jane E.;
Yuan, Xiaomeng;
Wang, Fang;
Pan, Haitao;
Graff, J. Carolyn;
Murphy, Laura;
Rupff, Rebecca;
Russell, Kathryn;
Wang, Winfred;
Estepp, Jeremie H.;
Hankins, Jane S.;
Porter, Jerlym S.;
Jacola, Lisa M.

Publication type:

Article

The Case for Pharmacogenetics‐Guided Prescribing of Codeine in Children.

Published in:

Clinical Pharmacology & Therapeutics, 2019, v. 105, n. 6, p. 1300, doi. 10.1002/cpt.1260

By:

Gammal, Roseann S.;
Caudle, Kelly E.;
Haidar, Cyrine E.;
Crews, Kristine R.;
Quinn, Charles T.;
Wang, Winfred C.;
Hankins, Jane S.;
Gaedigk, Andrea;
Prows, Cynthia A.;
Taylor, Annette K.;
Klein, Teri E.;
Sangkuhl, Katrin

Publication type:

Article

Assessment of Personal Medical History Knowledge in Adolescents with Sickle Cell Disease: A Pilot Study.

Published in:

Journal of Clinical Outcomes Management, 2016, v. 23, n. 6, p. 251

By:

Zhao, Mimi S.;
Johnson, Margery;
Pullen, Amanda;
Russell, Kathryn M.;
Wesley, Kimberly M.;
Hankins, Jane S.;
Porter, Jerlym S.

Publication type:

Article

Erratum to: Fast quantitative parameter maps without fitting: Integration yields accurate mono‐exponential signal decay rates (Magn Reson Med 2018;79:2978–2985).

Published in:

Magnetic Resonance in Medicine, 2019, v. 81, n. 2, p. 1470, doi. 10.1002/mrm.27405

By:

Song, Ruitian;
Loeffler, Ralf B.;
Holtrop, Joseph L.;
McCarville, M. Beth;
Hankins, Jane S.;
Hillenbrand, Claudia M.

Publication type:

Article

Fast quantitative parameter maps without fitting: Integration yields accurate mono‐exponential signal decay rates.

Published in:

Magnetic Resonance in Medicine, 2018, v. 79, n. 6, p. 2978, doi. 10.1002/mrm.26964

By:

Song, Ruitian;
Loeffler, Ralf B.;
Holtrop, Joseph L.;
McCarville, M. Beth;
Hankins, Jane S.;
Hillenbrand, Claudia M.

Publication type:

Article

Quantitative ultrashort echo time imaging for assessment of massive iron overload at 1.5 and 3 Tesla.

Published in:

Magnetic Resonance in Medicine, 2017, v. 78, n. 5, p. 1839, doi. 10.1002/mrm.26592

By:

Krafft, Axel J.;
Loeffler, Ralf B.;
Song, Ruitian;
Tipirneni‐Sajja, Aaryani;
McCarville, M. Beth;
Robson, Matthew D.;
Hankins, Jane S.;
Hillenbrand, Claudia M.

Publication type:

Article

Does fat suppression via chemically selective saturation affect R2*-MRI for transfusional iron overload assessment? A clinical evaluation at 1.5T and 3T.

Published in:

Magnetic Resonance in Medicine, 2016, v. 76, n. 2, p. 591, doi. 10.1002/mrm.25868

By:

Krafft, Axel J.;
Loeffler, Ralf B.;
Song, Ruitian;
Bian, Xiao;
McCarville, M. Beth;
Hankins, Jane S.;
Hillenbrand, Claudia M.

Publication type:

Article